A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532916



Internal ID20906277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43393407..43532860hg38UCSC Ensembl
chr18:40973372..41112825hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38139454
hg19139454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer